Natus Manufacturing Limited
12 devices · 33 adverse event reports · 0 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- Teca Elite S53153Electrode, Needle, Diagnostic Electromyograph7 reports
- Dantec 9013S0032Electrode, Needle, Diagnostic Electromyograph6 reports
- Dantec 9013S0042Electrode, Needle, Diagnostic Electromyograph4 reports
- Teca Elite S53156Electrode, Needle, Diagnostic Electromyograph3 reports
- Teca Elite 902-DMF25-SElectrode, Needle, Diagnostic Electromyograph3 reports
- Teca TP 902-DMG37-TPElectrode, Needle, Diagnostic Electromyograph3 reports
- Boject 9013S0422Electrode, Needle, Diagnostic Electromyograph2 reports
- Grass F-E2-48Electrode, Cutaneous1 report
- Myoject MJT-3726-LLElectrode, Needle, Diagnostic Electromyograph1 report
- Clavis 9015A0012Amplifier, Physiological Signal1 report
- Keypoint 9031E0722Stimulator, Electrical, Evoked Response1 report
- Grass® MR Conditional/CT Cup Electrodes MRARR27-59Electrode, Cutaneous1 report